Drug recall
Red Blood Cells, Leukocytes Reduced
FDA recall event 81661 · Class II, Class III · Good Samaritan Hospital Laboratory & Blood Donor Center,The
Key facts
| Event ID | 81661 |
|---|---|
| Recall numbers | B-0183-2019, B-0184-2019 |
| Recalling firm | Good Samaritan Hospital Laboratory & Blood Donor Center,The |
| Product type | Biologics |
| Products | Red Blood Cells, Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Red Blood Cells, not prepared in accordance with product specifications, were distributed. |
| Initiation date | Oct 2, 2018 |
| Report date | Dec 12, 2018 |
| Termination date | Dec 3, 2018 |
| City | Lebanon |
| State | PA |
| Country | United States |
| FEI number | 1000121175 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: